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Arabinoxylans (AXs) are complex polysaccharides with varying arabinose substitution patterns that affect their structural properties and self-assembly behaviors. In this study, we selected two sorghum varieties (S2 and S13) from a pool of 18 representative varieties, based on their distinct hemicellulose compositions. Techniques such as arabinoxylan-directed monoclonal antibodies (mAbs), High-Performance Anion-Exchange Chromatography (HPAEC), and 2-D HSQC NMR showed that S13 hemicellulose was of higher Ara/Xyl ratio of 0.22, compared to 0.09 in S2, which should be accounting for relatively high and low branching degrees of xylans. To gain deeper insights into the influence of arabinose side chains on xylan macromolecules, we measured and compared the morphology and self-assembly behaviors of nanoparticles from both varieties. Our findings indicate that nanoparticles from S2 were more slender and tended to assemble in a parallel orientation, while those from S13 displayed a vertical or disordered arrangement. By employing confined evaporation-induced self-assembly (C-EISA), we explored the self-assembly behavior of nanoparticles from each variety, and S13 nanoparticles in particular exhibited greater branching and distinct helical structures. These findings thus extend our understanding of the relationship between hemicellulose structure and its functional applications, offering insight for developing novel materials for drug delivery, biosensors, and other emerging applications.
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http://dx.doi.org/10.1016/j.carbpol.2025.123874 | DOI Listing |
Langmuir
September 2025
School of Light Industry Science and Engineering, Beijing Technology and Business University, Beijing 100048, People's Republic of China.
The study of the self-assembly of surfactants in aqueous solutions, though a traditional field, remains fascinating and full of novelty. In this article, the anionic perfluorodecanoic acid surfactant (PFA) is separately complexed with three hydroxyalkylamines (monoethanolamine (MEA), diethylamine (DEA), and triethanolamine (TEA)) in aqueous solutions. The transformation of aggregate morphologies from spherical unilamellar to nanotubes and then to spherical bilamellar is observed at room temperature, which is confirmed by cryo-transmission electron microscopy (cryo-TEM).
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Department of Materials Science and Engineering, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Republic of Korea.
Cyclic peptides (CPs) are versatile building blocks whose conformational constraints foster ordered supramolecular architectures with potential in biomedicine, nanoelectronics, and catalysis. Herein, we report the development of biomimetic antifreeze materials by conjugating CPs bearing ice-binding residues to 4-arm polyethylene glycol (PEG) via click chemistry. The concentration-dependent self-assembly of these CP-PEG conjugates induces programmable morphological transitions, forming nanotube networks above the critical aggregation concentration (CAC) and two-dimensional nanosheet networks near the CAC.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
Department of Chemistry and Biochemistry, Miami University, 651 E High St, Oxford, OH, 45056, USA.
Photodegradable nanoparticles with sphere, worm, and vesicle morphologies were synthesized following polymerization induced self-assembly (PISA), incorporating a photoresponsive phenyl vinyl ketone (PVK) block and a nonphoto responsive 2-hydroxypropyl methacrylamide (HPMA) block. The photodegradation of nanoparticles under UV revealed that the initial shapes of sphere and vesicle particles are retained even until 7 h and after 24 h of photo-induced degradation, respectively, despite a significant reduction in molecular weight (M). This could be due to the assembly of degraded PVK fragments in the hydrophobic region, maintaining the relative hydrophilic to hydrophobic ratio.
View Article and Find Full Text PDFAdv Sci (Weinh)
September 2025
Department of Chemistry, Gyeongsang National University, Jinju, 52828, South Korea.
Patchy nanoparticles (NPs) enable directional interactions and dynamic structural transformations, yet controlling polymeric patch formation with high spatial precision remains a significant challenge. Here, a thermally driven approach is presented to forming polystyrene (PS) patches on low-curvature facets of anisotropic gold nanocubes (NCs) using a single polymer component. Heating in DMF above 90 °C triggers selective desorption of PS chains from high-curvature edges and vertices via Au─S bond dissociation, followed by migration and deposition into rounded patches on flat surfaces.
View Article and Find Full Text PDFACS Omega
September 2025
Department of Chemistry, American University of Beirut, P.O. Box 11-0236, Riad El-Solh, 1107 2020 Beirut, Lebanon.
Fractal growth in reaction-diffusion frameworks (RDF) offers a powerful paradigm for understanding self-assembly in chemical and materials systems. However, its connection to diffusion-limited aggregation (DLA) remains underexplored. Here, we present the first quantitative demonstration of RDF-driven fractal crystallization of benzoic acid (BA), revealing a direct correlation among fractal dimension, diffusion rate, and gel-matrix chemistry.
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